CLASS II ONGOING Drug recall · Reported 3 Dec 2025 · FDA Enforcement Report

Walgreens Saline Nasal Spray With Xylitol recalled

Medical Products Laboratories is recalling Walgreens Saline Nasal Spray With Xylitol, distributed nationwide in the US. The recall was initiated on 12 Nov 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot#: 71409, Expires: 02/28/2027; 71861, Expires: 08/31/2027.
Quantity recalled41,328 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0179-2026
FDA event ID
97949
Recalling firm
Medical Products Laboratories, Philadelphia, PA
Classification
Class II
Status
Ongoing
Recall initiated
12 Nov 2025
FDA classified
21 Nov 2025
Reported
3 Dec 2025
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Sterility
Drug class
Nasal Sprays

Timeline

12 Nov 2025Recall initiated by company
21 Nov 2025Classified by FDA+9 days
3 Dec 2025Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Microbial contamination of a non-sterile product - microorganism found to be pseudomonas lactis

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

Walgreens Saline Nasal Spray WITH XYLITOL, 1.5 oz (45mL) bottle, DISTRIBUTED BY: WALGREEN CO., 200 WILMOT RD., DEERFIELD, IL 60015, NDC 0363-3114-01

Where it was distributed

Nationwide USA

Nationwide

Stores named: Walgreens

Questions about this recall

Why was it recalled?

Microbial contamination of a non-sterile product - microorganism found to be pseudomonas lactis

Which lots are affected?

Lot#: 71409, Expires: 02/28/2027; 71861, Expires: 08/31/2027.

Where was it sold?

Nationwide USA

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.